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Epcoritamab in relapsed/refractory large B-cell lymphoma: 2-year follow-up from the pivotal EPCORE NHL-1 trial

  • Catherine Thieblemont,
  • Yasmin H. Karimi,
  • Herve Ghesquieres,
  • Chan Y. Cheah,
  • Michael Roost Clausen,
  • David Cunningham,
  • Wojciech Jurczak,
  • Young Rok Do,
  • Robin Gasiorowski,
  • David John Lewis,
  • Tae Min Kim,
  • Marjolein van der Poel,
  • Michelle Limei Poon,
  • Tatyana Feldman,
  • Kim M. Linton,
  • Anna Sureda,
  • Martin Hutchings,
  • Minh H. Dinh,
  • Nurgul Kilavuz,
  • David Soong,
  • Thomas Mark,
  • Mariana Sacchi,
  • Tycel Phillips,
  • Pieternella J. Lugtenburg

摘要

Primary results (median follow-up, 10.7 months) from the pivotal EPCORE® NHL-1 study in relapsed or refractory (R/R) large B-cell lymphoma (LBCL) demonstrated deep, durable responses with epcoritamab, a CD3xCD20 bispecific antibody, when used as monotherapy. We report long-term efficacy and safety results in patients with LBCL (N = 157; 25.1-month median follow-up). As of April 21, 2023, overall response rate was 63.1% and complete response (CR) rate was 40.1%. Estimated 24-month progression-free survival (PFS) and overall survival (OS) rates were 27.8% and 44.6%, respectively. An estimated 64.2% of complete responders remained in CR at 24 months. Estimated 24-month PFS and OS rates among complete responders were 65.1% and 78.2%, respectively. Of 119 minimal residual disease (MRD)-evaluable patients, 45.4% had MRD negativity, which correlated with longer PFS and OS. CR rates were generally consistent across predefined subgroups: 36% prior chimeric antigen receptor (CAR) T-cell therapy, 32% primary refractory disease, and 37% International Prognostic Index ≥3. The most common treatment-emergent adverse events were cytokine release syndrome (51.0%), pyrexia (24.8%), fatigue (24.2%), and neutropenia (23.6%). These results underscore the long-term benefit of epcoritamab for treating R/R LBCL with deep responses across subgroups, including patients with hard-to-treat disease and expected poor prognosis (ClinicalTrials.gov Registration: NCT03625037).